POAG Flashcards

1
Q

What happens to IOP right after a CRVO?

A

Temporary hypotony
(Eyes with elevated IOPs are at risk of developing CRVO. Elevated IOP in the fellow eye of an eye affected with RVO must kept low as reasonably possible.

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2
Q

Histologially, the PXE material resembles what?

A

Amyloid

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3
Q

When dilated, pigment deposits can be seen on the zonular fibers and both the anterior and posterior lens capsule near the equator of the lens?

A

Zentmayer’s line

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4
Q

PXE gl is u/l or b/l?

A

Monocular or binocular with varying degrees of asymmetry. Often the d/o is clinically apparent in only 1 eye, but other eye develops later.

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5
Q

Iris transillumination defects at the pupillary margin vs iris mid periphery?

A

Margin - PXE

Midperiphery - Pigmentary GL

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6
Q

What percentage of patients with PDS develop GL?

A

25-50%

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7
Q

What is the demographic of PDS?

A

White males with myopia btwn age 20 to 50 yrs.

Affected females tend to be older than affected males.

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8
Q

Which POAG has the widest fluctuation in IOP?

A

PDS - can exceed 50 mm Hg in untreated eyes.

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9
Q

The lack of KP helps distinguish what types of GL?

A

Distinguish phacolytic gl from phacoanaphylaxis.

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10
Q

The presense of KP and a miotic pupil suggest what as the cause of increased IOP?

A

Iritis

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11
Q

When does Ghost cell gl develop?

A

1-3 months following VH.

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12
Q

Trabeculitis is what and occurs in what GL?

A

KP on the TM - Posner-Schlossman

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13
Q

Which study DID NOT look at FHx as a risk factor for development of GL?

A

OHTS

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